(Q30050619)

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

Rossella Tupler

3

0 references

Davide Gabellini

object named as

Davide Gabellini

series ordinal

1

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author name string

Michael R. Green

series ordinal

2

1 reference

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

language of work or name

English

0 references

publication date

August 2002

1 reference

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

1 reference

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

volume

110

1 reference

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

issue

3

1 reference

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

25 May 2017

page(s)

339-348

1 reference

https://doi.org/10.1016%2FS0092-8674%2802%2900826-7

Adenine nucleotide translocase-1, a component of the permeability transition pore, can dominantly induce apoptosis

25 May 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1 reference

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7 January 2021

c-Myc target gene specificity is determined by a post-DNAbinding mechanism

1 reference

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7 January 2021

Characterization of the chicken beta-globin insulator

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

The myocardial expression of the adenine nucleotide translocator isoforms is specifically altered in dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

An approach to correlate tandem mass spectral data of peptides with amino acid sequences in a protein database

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Nucleolin is one component of the B cell-specific transcription factor and switch region binding protein, LR1.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Role of adenine nucleotide translocator 1 in mtDNA maintenance

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Chromatin components as part of a putative transcriptional repressing complex

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

44th ENMC International Workshop: Facioscapulohumeral Muscular Dystrophy: Molecular Studies 19-21 July 1996, Naarden, The Netherlands

1 reference

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7 January 2021

Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Mechanisms of silencing in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Achieving efficient delivery of morpholino oligos in cultured cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Mapping Polycomb-repressed domains in the bithorax complex using in vivo formaldehyde cross-linked chromatin

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Limitations of silencing at native yeast telomeres

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Silent domains are assembled continuously from the telomere and are defined by promoter distance and strength, and by SIR3 dosage

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facioscapulo human muscular dystrophy. A potential target for pharmacological treatment?

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Identification of nucleolin as a glucocorticoid receptor interacting protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

DNA‐fragmentation and expression of apoptosis‐related proteins in muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Unlocking the mechanisms of transcription factor YY1: are chromatin modifying enzymes the key?

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

HMG1 and 2, and related 'architectural' DNA-binding proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

High affinity YY1 binding motifs: identification of two core types (ACAT and CCAT) and distribution of potential binding sites within the human beta globin cluster

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

Nucleolin, a novel partner for the Myb transcription factor family that regulates their activity

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2802%2900826-7

7 January 2021

10.1016/S0092-8674(02)00826-7

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/syzhnfphhndw3btu66lu5wyjeq

30 July 2022

mapped directly with Wikidata item

Fatcat ID

release_syzhnfphhndw3btu66lu5wyjeq

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/syzhnfphhndw3btu66lu5wyjeq

30 July 2022

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

3237839

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3237839

PubMed publication ID

1 reference

https://api.fatcat.wiki/v0/release/syzhnfphhndw3btu66lu5wyjeq

30 July 2022